AeroGear™

GUDID 50604351895107

MONAGHAN MEDICAL CORPORATION

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• Primary Device ID: 50604351895107
• NIH Device Record Key: 63b7fa3a-a01f-4812-9217-fc1bcf40dffe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AeroGear™
• Version Model Number: Asthma Action Kit, cs/10
• Company DUNS: 056332380
• Company Name: MONAGHAN MEDICAL CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com
• Phone: 518-561-7330
• Email: customerservice@monaghanmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00604351895102 [Primary]
GS1	50604351895107 [Package]; Contains: 00604351895102; Package: [10 Units]; In Commercial Distribution

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-12-19

Devices Manufactured by MONAGHAN MEDICAL CORPORATION

• 50604351504122 - Aerochamber Plus® Flow-Vu®: 2024-03-11 AC Plus, Flow-Vu aVHC, Intermediate Mask, Retail - 50412
• 00604351500129 - Aerochamber Plus® Flow-Vu®: 2023-11-22 AC+FV aVHC Mouthpiece Retail - 50012
• 50604351501121 - Aerochamber Plus® Flow-Vu®: 2023-11-22 AC Plus, Flow-Vu aVHC, Small Mask, Retail - 50112
• 50604351502128 - Aerochamber Plus® Flow-Vu®: 2023-11-22 AC Plus, Flow-Vu aVHC, Medium Mask, Retail - 50212
• 50604351503125 - Aerochamber Plus® Flow-Vu®: 2023-11-22 AC Plus, Flow-Vu aVHC, Large Mask, Retail - 50312
• 50604351601258 - AeroEclips*BAN*: 2023-09-14 AE II BAN with Universal Tubing & Filtered Mouthpiece Kit, cs/25
• 00604351602250 - AeroEclipse* BAN*: 2023-09-14 AE II BAN with EZ Twist Tubing & Filtered Mouthpiece Kit, cs/25
• 50604351600527 - Filtered Mouthpiece: 2023-09-01